ENST00000380649.8:c.1105G>A
MANE Select
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ENSP00000370023.3:p.Ala369Thr
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ENST00000492433.2:c.1105G>A
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ENSP00000438039.2:p.Ala369Thr
|
|
ENST00000643057.1:c.*996G>A
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ENSP00000493761.1:n.*996G>A
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ENST00000643063.1:c.*151G>A
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ENSP00000495353.1:n.*151G>A
|
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ENST00000643233.1:c.*996G>A
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ENSP00000493880.1:n.*996G>A
|
|
ENST00000644428.1:c.1105G>A
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ENSP00000495560.1:p.Ala369Thr
|
|
ENST00000645274.1:c.1000G>A
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ENSP00000493996.1:p.Ala334Thr
|
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ENST00000646031.1:c.464G>A
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|
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ENST00000646483.1:c.971G>A
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ENSP00000496185.1:n.971G>A
|
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ENST00000380649.7:c.1105G>A
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ENSP00000370023.3:p.Ala369Thr
|
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NM_000182.4:c.1105G>A
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NP_000173.2:p.Ala369Thr
|
|
NM_000182.5:c.1105G>A
MANE Select
|
NP_000173.2:p.Ala369Thr
|
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